Precise surface functionalization of PLGA particles for human T cell modulation.

The biofunctionalization of synthetic materials has extensive utility for biomedical applications, but approaches to bioconjugation typically show insufficient efficiency and controllability. We recently developed an approach by building synthetic DNA scaffolds on biomaterial surfaces that enables the precise control of cargo density and ratio, thus improving the assembly and organization of functional cargos. We used this approach to show that the modulation and phenotypic adaptation of immune cells can be regulated using our precisely functionalized biomaterials. Here, we describe the three key procedures, including the fabrication of polymeric particles engrafted with short DNA scaffolds, the attachment of functional cargos with complementary DNA strands, and the surface assembly control and quantification. We also explain the critical checkpoints needed to ensure the overall quality and expected characteristics of the biological product. We provide additional experimental design considerations for modifying the approach by varying the material composition, size or cargo types. As an example, we cover the use of the protocol for human primary T cell activation and for the identification of parameters that affect ex vivo T cell manufacturing. The protocol requires users with diverse expertise ranging from synthetic materials to bioconjugation chemistry to immunology. The fabrication procedures and validation assays to design high-fidelity DNA-scaffolded biomaterials typically require 8 d.

Flexible thermal conductive Al2O3@siloxane composite with rapid self-healing property based on carboxyl-amine dynamic reversible bonds.

Thermal interface materials (TIMs) are one of the efficacious ways to alleviate the heat accumulation problem of microelectronics devices. However, conventional TIMs based on polydimethylsiloxane (PDMS) always suffer from mechanical damage, leading to shortened service life or loss of thermal conductivity. In this work, we fabricated a high-thermal conductivity and fast self-healable Al2O3@siloxane composite by hydrosilylation reaction. The siloxane matrix consisted of thermosetting silicone rubber matrix (SR) and heat reversibility matrix (SCNR); the SR was synthesized via hydrosilylation between silicon hydrogen bond and vinyl, the SCNR was fabricated by thermal-curing between amino and carboxyl functionalized PDMS. Different sized spherical Al2O3 fillers were introduced into the SR/SCNR matrix system to construct the Al2O3@SR/SCNR composites. By adjusting the ratio of SR/SCNR, the obtained composites can achieve flexibility, self-healing and high filling simultaneously. It is notable that the self-healing efficiency of the composite is high, up to 95.6% within 3 minutes with 6.7 wt% mass ratio of SCNR/SR; these fast self-healing behaviors benefit from the assistance of thermal diffusion by 3D heat conduction pathways on the rearrangement of the dynamic cross-linked network. The resultant composites also exhibited the optimal thermal conductivity of 5.85 W mK-1. This work provides a novel approach for constructing longer service life and high thermal conductivity multifunctional TIM based PDMS.

Flexible Fiber Membrane Based on Carbon Nanotube and Polyurethane with High Thermal Conductivity.

The development of high thermally conductive polymer composites with low filler content remains challenging in the field of thermal interface materials (TIMs). Herein, we fabricated a series of flexible fiber membranes (TMMFM) with high thermally conductive based on thermoplastic polyurethane (TPU) and acidified multiwalled carbon nanotubes (a-MWCNTs) via electrospinning and ultrasonic anchoring method. The SEM and TEM results demonstrated that the a-MWCNTs aligned along the fiber orientation in the membrane and anchored on the membrane surface strongly, which can establish the heat conduction path both in the horizontal and vertical directions. With the incorporation of 10 wt% a-MWCNTs, the horizontal direction (λ∥) and vertical direction (λ⊥) thermal conductivity value of TMMFM-5 was 3.60 W/mK and 1.79 W/mK, respectively, being 18 times and 10 times higher compared to pure TPU fiber membranes. Furthermore, the TMMFM maintained favorable flexibility of the TPU matrix because the small amount of a-MWCNTs only slightly hinders the mobility of the TPU molecular chain. The performance of the obtained TMMFM unveils their potential as a promising choice of flexible TIMs.

A Novel Method to Prepare Transparent, Flexible and Thermally Conductive Polyethylene/Boron Nitride Films.

The high thermal conductivity and good insulating properties of boron nitride (BN) make it a promising filler for high-performance polymer-based thermal management materials. An easy way to prepare BN-polymer composites is to directly mix BN particles with polymer matrix. However, a high concentration of fillers usually leads to a huge reduction of mechanical strength and optical transmission. Here, we propose a novel method to prepare polyethylene/boron nitride nanoplates (PE/BNNPs) composites through the combination of electrostatic self-assembly and hot pressing. Through this method, the thermal conductivity of the PE/BNNPs composites reach 0.47 W/mK, which gets a 14.6% improvement compared to pure polyethylene film. Thanks to the tight bonding of polyethylene with BNNPs, the tensile strength of the composite film reaches 1.82 MPa, an increase of 173.58% compared to that of pure polyethylene film (0.66 MPa). The fracture stress was also highly enhanced, with an increase of 148.44% compared to pure polyethylene film. Moreover, the addition of BNNPs in PE does not highly reduce its good transmittance, which is preferred for thermal management in devices like light-emitting diodes. This work gives an insight into the preparation strategy of transparent and flexible thermal management materials with high thermal conductivity.

Tough and durable hydrogels with robust skin layers formed via soaking treatment.

Recent progress has seen significant advances in the mechanical performances of synthetic hydrogels. However, the mechanics of hydrogels usually suffer drastic degradation under repetitive mechanical and complicated environmental loadings. Here, we fabricate a class of biocompatible layered poly(vinyl alcohol) hydrogels by simply soaking a preformed poly(vinyl alcohol) gel in sodium silicate. The resulting hydrogels exhibit a combination of superior mechanical performances and good biocompatibility, along with exceptional chemical robustness. The layered structure is composed of a compact cover layer and a porous center layer. Both layers are composed of poly(vinyl alcohol). The network in the cover is crosslinked by ordered polarized H-bonds with swelling stability, while the porous center confines a large volume of interstitial water. The structural and crosslinking metric confers the hydrogels with capabilities to tolerate complicated mechanical and environmental loads. The optimized gel is tough (fracture energy >10 kJ m-2) and strong (fracture stress ≈ 5 MPa). The strengthening mechanism can be correlated to the layered structure, which causes the impeded flow of interstitial water. Their mechanical performance is maintained in strong acidic/alkaline, and concentrated electrolytes, and in the presence of salting-in and H-bond-breaking reagents even at elevated temperatures. We speculate that the dipole-dipole pairings of Oδ--Hδ+ Oδ--Hδ+ in the cover layer probably generate hydrophobic microdomains. This swelling-resistant interaction may protect the hydrogels from swelling in complex aqueous envrionments. We also discuss the possible mechanism of the formation of layered structures and their crosslinkings.